What is Chronic Pain

Chronic pain becomes chronic when it persists longer than 6 months and is resistant to medical management. Millions of Americans are chronic pain patients and some exper...

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Discussion:
Greetings or Got A Name For It?
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Hello fellow CPers. Just found this forum yesterday while doing some research. That research led me to writing the following this morning which sums up where I'm at and what I deal with:



Got A Name For It?

After tons of research, I have finally discovered where my lifelong joint pain is coming from. Well, at least I found a name for it:
Chronic Tendonosis.
Not tendonitis. Tendonitis suggests inflamation in the tendons. Tendonosis suggests deterioration or degeneration of the tendons.
And, I've been dealing with this for 25 years or so. It goes back to when I was 15. I grew a foot in a year. My tendons globally did not keep up. One other thing I remembered once I discovered tendonosis is that I was diagnosed with Osgood-Schlatters back then. That's caused by growing too fast and having the tendon that holds your kneecaps on get inflamed and become a painful bump where it connects to the tibia.

And, it never healed. None of it.

I gotta tell ya, it's such a relief to me to finally be able to name the joint pain. For awhile there, I thought I was going crazy. Nope.
It was astounding. I was looking at a diagram of the human body and where all the major tendons are. As I went down the body, I was like, check, check, got it, check, yep, that one too, check. Shoulders, elbows, hands, fingers, most of my spine, occasionally my hips, especially the knees, and feet. As I looked at the diagram of the feet, I saw that we have two huge tendons that come down from the sides of the ankle and around the sides of the feet. These help hold the arch of the foot up. And, when I wake up in the morning and put pressure on my feet, the eye-crossing pain is coming directly from them.

It's like I can actually see, or visualize rather, the source of all of this now. It's a huge weight lifted off my mind.

Now, knowing this, changes nothing. If it hasn't gotten better (and only gotten worse as I've aged - 40 now) I doubt it's ever going to improve. It does change the way I think about it though. I've been thinking I have arthritis all this time. Which reminds me; it's no wonder all that glucosamine I've been taking hasn't helped one bit. It's not been the cartilage afterall. Duh. I guess, in my mind, thinking that if I do too much with my joints, bend too much, over stress them too much, that I would do more damage. Now that I know it's my tendons, I think I may function a little differently. I suppose the chance of me tearing a tendon is good, but still, I might not have to baby my body so much now. I'm sure that hasn't helped me much.

Now I need to find a way to strengthen the muscles around my offending joints. Help support the tendons a bit more. This is a catch-22 though. I cannot run. I can't do any high impact excersise at all. It just hurts too f*cking much. I can swim. I need to look into yoga. If I remember correctly, my friend is going to point me in the right direction with that.

I just have to be careful. Having degenerative disc disease in my back ups the stakes. When my back takes a shit, it's all over. (Which it's wont to do every six months or so...)

Now, all I need to do is figure out why I have begun having constantly pinched nerves in my uppper back and neck and I'll be all groovy. More or less. Heh.

Chronic Tendonosis. Who'da thunk it? Better question is; why didn't my doctor?


And that's that. To top all that painwise, I also live with Hydradenitis Suppurativa. Something most folks have never heard of. It's one painful bitch of a thing.
So yeah, I'm a mess. But, thanks to modern medicine, I function a bit more like a normal human being and try to stay positive. Which is quite a feat for someone who is pessimistic by nature.

I've been doing a lot of reading of posts here since I found it and have found all kinds of good info and folks who seem cool. So, I thought, why not. Join. So, howdy.
Posted on 11/19/08, 03:11 pm
27 Replies | Most Recent Add Your Reply
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Reply #21 - 11/21/08  5:04pm
" Thanks Doc. I'll look into that. First I need to figure out how long my insurance will last and all that mess that comes when you lose your job. "
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Reply #22 - 11/21/08  5:18pm
" Yes, they offered it. I'll have to weight the benefits of what costs more, that, or my scripts outright. I don't even know if cobra covers scripts. I've never had to use it before.

And thanks for the laugh, "chick who really loves that show". I need all of them I can get right now. "
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Reply #23 - 11/21/08  6:33pm
" Yep. I just looked at the paperwork. $387 a month. Holy Gopherburgers Batman!! But, without insurance, I croak. So, I gotta find a way to pay it. "
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Reply #24 - 11/22/08  7:54am
" Holy crap!! There has got to be a better answer than that!! Hopefully, this is an area that Obama can do something about.
I am disabled (on disability) so I can have Medicare (kicks in after 2 yrs), but am lucky to have a husband with great ins.
Do you feel that you can get another job? Of course, even then they would hit you with "pre-existing" (I have worked with insurance for many years)
I can't imagine you being able to work with all that is going on,---would you qualify for any of the state programs? Perhaps state funded "High Risk" insurance would be cheaper for you than the Cobra coverage. That just sucks!
Good luck to you, Joe! Judy "
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Reply #25 - 11/22/08  8:58am
" I'm baffled by it all Judy. I'll look into what your telling me here though. I'm still kinda shellshocked at this point. "
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Reply #26 - 11/04/09  11:38pm
" Hey Joe, Any luck finding insurance. My cobra was to expensive for me too. I have no income can't work at all. My dad pays for my medicines and doctor visits. I got a discount prescription card on the net which helps alot with meds as long as I use Walmart. Hope things are working out for you. My tendinosis is getting worse daily. Wish you the best. "
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Reply #27 - 11/04/09  11:51pm
" Welcome Joe, I didn't read through all the replies, but I was thinking along the same lines as Orchid, I too have Ehlers Danlos Syndrome Hypermobility type and kyphosis, degenerative scoliosis, etc...
When my spine specialist sent me to see a genetic specialist and they diagnosed me with EDS I was so relieved to have a name for it, yea I'm not crazy!!!! Unfortunately there is no cure but I am lucky to have a family practice Dr and specialist who work well together to control my pain and try and keep me as upright for as long as possible. I've lost 4 inches in height in the last 8 years and things are definately not going to get better.
Again welcome and good luck! "

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